Canonical Allele Identifier: CA1220396657
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728570_215728572delinsTAA , CM000663.2:g.215728570_215728572delinsTAA GRCh38
NC_000001.10:g.215901912_215901914delinsTAA , CM000663.1:g.215901912_215901914delinsTAA GRCh37
NC_000001.9:g.213968535_213968537delinsTAA NCBI36
NG_009497.1:g.699825_699827delinsTTA
NG_009497.2:g.699877_699879delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-188_11712-186delinsTTA MANE Select ENSP00000305941.3:n.11712-188_11712-186delinsTTA
ENST00000674083.1:c.11712-188_11712-186delinsTTA ENSP00000501296.1:n.11712-188_11712-186delinsTTA
ENST00000307340.7:c.11712-188_11712-186delinsTTA ENSP00000305941.3:n.11712-188_11712-186delinsTTA
NM_206933.2:c.11712-188_11712-186delinsTTA NP_996816.2:n.11712-188_11712-186delinsTTA
NM_206933.3:c.11712-188_11712-186delinsTTA NP_996816.2:n.11712-188_11712-186delinsTTA
NM_206933.4:c.11712-188_11712-186delinsTTA MANE Select NP_996816.3:n.11712-188_11712-186delinsTTA